Chylomicron retention disease Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Chylomicron retention disease (CRD) is a type of familial hypocholesterolemia characterized by malnutrition, failure to thrive, growth failure, vitamin E deficiency and hepatic, neurologic and ophthalmologic complications. (Orphanet Rare Disease Ontology, Orphanet_71)
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1 genes associated with the Chylomicron retention disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
SAR1B secretion associated, Ras related GTPase 1B